@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_head
{
this:
np:hasAssertion
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion
;
np:hasProvenance
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion
a
np:Assertion
.
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_provenance
a
np:Provenance
.
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion
{
miriam-gene:8647
a
ncit:C16612
.
lld:C0019196
a
ncit:C7057
.
dgn-gda:DGN0cc3d9f3b8cbbd808de27264b37bba6f
sio:SIO_000628
miriam-gene:8647
,
lld:C0019196
;
a
sio:SIO_001121
.
}
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_provenance
{
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion
dcterms:description
"[A common variant of BSEP (p.V444A) is now a well-established susceptibility factor for acquired cholestasis and recent evidence suggests that the same variant also influences the therapeutic response and disease progression of viral hepatitis C. Studies in large independent cohorts are now needed to confirm the relevance of p.V444A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21320040
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}